Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens

Toll-Like Receptors

Takeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141126 · Cited by 6,143 · see citing works

The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5

Hayashi, F., Smith, K. D., Ozinsky, A., Hawn, T. R., Yi, E. C., Goodlett, D. R., Eng, J. K., Akira, S., Underhill, D. M., & Aderem, A. A. (2001) · Nature · doi:10.1038/35074106 · Cited by 3,605 · see citing works

An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System

Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910 · see citing works

Recognition of microorganisms and activation of the immune response

Medzhitov, R. (2007) · Nature · doi:10.1038/nature06246 · Cited by 2,862 · see citing works

Dendritic cells express tight junction proteins and penetrate gut epithelial monolayers to sample bacteria

Rescigno, M., Urbano, M., Valzasina, B., Francolini, M., Rotta, G., Bonasio, R., Granucci, F., Kraehenbuhl, J.-P., & Ricciardi‐Castagnoli, P. (2001) · Nature Immunology · doi:10.1038/86373 · Cited by 2,554 · see citing works

Commensal Host-Bacterial Relationships in the Gut

Hooper, L. V., & Gordon, J. I. (2001) · Science · doi:10.1126/science.1058709 · Cited by 2,362 · see citing works

A microbial symbiosis factor prevents intestinal inflammatory disease

Mazmanian, S. K., Round, J. L., & Kasper, D. L. (2008) · Nature · doi:10.1038/nature07008 · Cited by 2,340 · see citing works

Symbiotic bacteria direct expression of an intestinal bactericidal lectin

Cash, H. L., Whitham, C. V., Behrendt, C. L., & Hooper, L. V. (2006) · Science · doi:10.1126/science.1127119 · Cited by 1,432 · see citing works

The Toll-like receptor 2 is recruited to macrophage phagosomes and discriminates between pathogens

Underhill, D. M., Ozinsky, A., Hajjar, A. M., Stevens, A. M., Wilson, C. B., Bassetti, M., & Aderem, A. A. (1999) · Nature · doi:10.1038/44605 · Cited by 1,369 · see citing works

Cooperation of Toll-like receptor signals in innate immune defence

Trinchieri, G., & Sher, A. (2007) · Nature reviews. Immunology · doi:10.1038/nri2038 · Cited by 1,357 · see citing works

Crystal Structure of the TLR1-TLR2 Heterodimer Induced by Binding of a Tri-Acylated Lipopeptide

Jin, M. S., Kim, S. E., Heo, J. Y., Lee, M. E., Kim, H. M., Paik, S., Lee, H., & Lee, J. (2007) · Cell · doi:10.1016/j.cell.2007.09.008 · Cited by 1,352 · see citing works

Cutting Edge: Bacterial Flagellin Activates Basolaterally Expressed TLR5 to Induce Epithelial Proinflammatory Gene Expression

Gewirtz, A. T., Navas, T. A., Lyons, S., Godowski, P. J., & Madara, J. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.4.1882 · Cited by 1,345 · see citing works

Antagonistic activities of lactobacilli and bifidobacteria against microbial pathogens

Servin, A. L. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2004.01.003 · Cited by 1,234 · see citing works

Glycan foraging in vivo by an intestine-adapted bacterial symbiont

Sonnenburg, J. L., Xu, J., Leip, D. D., Chen, C.-H., Westover, B. P., Weatherford, J., Buhler, J. D., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1109051 · Cited by 1,184 · see citing works

Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut

Artis, D. (2008) · Nature reviews. Immunology · doi:10.1038/nri2316 · Cited by 1,136 · see citing works

Secretion of microbicidal α-defensins by intestinal Paneth cells in response to bacteria

Ayabe, T., Satchell, D. P., Wilson, C. L., Parks, W. C., Selsted, M. E., & Ouellette, A. J. (2000) · Nature Immunology · doi:10.1038/77783 · Cited by 1,060 · see citing works

A Continuum of Anionic Charge: Structures and Functions of d -Alanyl-Teichoic Acids in Gram-Positive Bacteria

Neuhaus, F. C., & BADDILEY, J. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.4.686-723.2003 · Cited by 1,035 · see citing works

Genes and Molecules of Lactobacilli Supporting Probiotic Action

Lebeer, S., Vanderleyden, J., & De Keersmaecker, S. C. J. (2008) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00017-08 · Cited by 1,013 · see citing works

DC-SIGN: escape mechanism for pathogens

van Kooyk, Y., & Geijtenbeek, T. B. H. (2003) · Nature reviews. Immunology · doi:10.1038/nri1182 · Cited by 930 · see citing works

Signalling pathways and molecular interactions of NOD1 and NOD2

Strober, W., Murray, P. J., Kitani, A., & Watanabe, T. (2005) · Nature reviews. Immunology · doi:10.1038/nri1747 · Cited by 856 · see citing works

Heteropolysaccharides from lactic acid bacteria

Vuyst, L. D., & Degeest, B. (1999) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.1999.tb00395.x · Cited by 840 · see citing works

IgA Response to Symbiotic Bacteria as a Mediator of Gut Homeostasis

Peterson, D. A., McNulty, N. P., Guruge, J. L., & Gordon, J. I. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.09.013 · Cited by 828 · see citing works

Soluble Proteins Produced by Probiotic Bacteria Regulate Intestinal Epithelial Cell Survival and Growth

Yan, F., Cao, H., Cover, T. L., Whitehead, R. H., Washington, M. K., & Polk, D. B. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.11.022 · Cited by 828 · see citing works

Selective probiotic bacteria induce IL-10–producing regulatory T cells in vitro by modulating dendritic cell function through dendritic cell–specific intercellular adhesion molecule 3–grabbing nonintegrin

Smits, H. H., Engering, A. J., van der Kleij, D., de Jong, E. C., Schipper, K., van Capel, T. M. M., Zaat, B. A. J., Yazdanbakhsh, M., Wierenga, E. A., & van Kooyk, Y. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.03.036 · Cited by 765 · see citing works

Intestinal Alkaline Phosphatase Detoxifies Lipopolysaccharide and Prevents Inflammation in Zebrafish in Response to the Gut Microbiota

Bates, J. M., Akerlund, J., Mittge, E., & Guillemin, K. J. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.10.010 · Cited by 752 · see citing works

The Plasticity of Dendritic Cell Responses to Pathogens and Their Components

Huang, Q., Liu, D., Majewski, P., Schulte, L. C., Korn, J. M., Young, R. A., Lander, E. S., & Hacohen, N. (2001) · Science · doi:10.1126/science.294.5543.870 · Cited by 747 · see citing works

Comparative genomic analysis of <i>Lactobacillus rhamnosus</i> GG reveals pili containing a human- mucus binding protein

Kankainen, M., Paulin, L., Tynkkynen, S., von Ossowski, I., Reunanen, J., Partanen, P., Satokari, R., Vesterlund, S., Hendrickx, A. P. A., Lebeer, S., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908876106 · Cited by 740 · see citing works

Structure and function of lipopolysaccharides

Erridge, C., Bennett‐Guerrero, E., & Poxton, I. R. (2002) · Microbes and Infection · doi:10.1016/s1286-4579(02)01604-0 · Cited by 682 · see citing works

Decreased Expression of Toll-Like Receptor-4 and MD-2 Correlates with Intestinal Epithelial Cell Protection Against Dysregulated Proinflammatory Gene Expression in Response to Bacterial Lipopolysaccharide

Abreu, M. T., Vora, P., Faure, E., Thomas, L. S., Arnold, E. T., & Arditi, M. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.3.1609 · Cited by 681 · see citing works

Extracellular MUC3 mucin secretion follows adherence of Lactobacillus strains to intestinal epithelial cells in vitro

Mack, D. R., Ahrné, S., Hyde, L., Wei, S. H., & Hollingsworth, M. A. (2003) · Gut · doi:10.1136/gut.52.6.827 · Cited by 666 · see citing works

Evasion of Toll-like receptor 5 by flagellated bacteria

Andersen‐Nissen, E., Smith, K. D., Strobe, K. L., Barrett, S. L. R., Cookson, B. T., Logan, S. M., & Aderem, A. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502040102 · Cited by 657 · see citing works

A Model of Host-Microbial Interactions in an Open Mammalian Ecosystem

Bry, L., Falk, P. G., Midtvedt, T., & Gordon, J. I. (1996) · Science · doi:10.1126/science.273.5280.1380 · Cited by 607 · see citing works

C-Type Lectin DC-SIGN Modulates Toll-like Receptor Signaling via Raf-1 Kinase-Dependent Acetylation of Transcription Factor NF-κB

Gringhuis, S. I., den Dunnen, J., Litjens, M., Hof, B. V. H., van Kooyk, Y., & Geijtenbeek, T. B. H. (2007) · Immunity · doi:10.1016/j.immuni.2007.03.012 · Cited by 588 · see citing works

TLR Signaling in the Gut in Health and Disease

Abreu, M. T., Fukata, M., & Arditi, M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.4453 · Cited by 577 · see citing works

S layer protein A of Lactobacillus acidophilus NCFM regulates immature dendritic cell and T cell functions

Konstantinov, S. R., Smidt, H., de Vos, W. M., Bruijns, S. C. M., Singh, S., Valence, F., Mollé, D., Lortal, S., Altermann, E., Klaenhammer, T. R., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810305105 · Cited by 568 · see citing works

Modulation of human dendritic cell phenotype and function by probiotic bacteria

Hart, A. L., Lammers, K., Brigidi, P., Vitali, B., Rizzello, F., Gionchetti, P., Campieri, M., Kamm, M. A., Knight, S. C., & Stagg, A. J. (2004) · Gut · doi:10.1136/gut.2003.037325 · Cited by 555 · see citing works

Pili in Gram-negative and Gram-positive bacteria — structure, assembly and their role in disease

Proft, T., & Baker, E. N. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8477-4 · Cited by 549 · see citing works

Exopolysaccharides from lactic acid bacteria: perspectives and challenges

Welman, A. D., & Maddox, I. S. (2003) · Trends in biotechnology · doi:10.1016/s0167-7799(03)00107-0 · Cited by 523 · see citing works

Mechanisms of cross hyporesponsiveness to toll-like receptor bacterial ligands in intestinal epithelial cells☆

Otte, J., Cario, E., & Podolsky, D. K. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.01.007 · Cited by 506 · see citing works

Toll‐like receptor 2‐dependent bacterial sensing does not occur via peptidoglycan recognition

Travassos, L. H., Girardin, S. E., Philpott, D. J., Blanot, D., Nahori, M., Werts, C., & Boneca, I. G. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400248 · Cited by 504 · see citing works

Probiotics and immunity

Borchers, A. T., Selmi, C. F., Meyers, F. J., Keen, C. L., & Gershwin, M. E. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-008-2296-0 · Cited by 502 · see citing works

A molecular sensor that allows a gut commensal to control its nutrient foundation in a competitive ecosystem

Hooper, L. V., Xu, J., Falk, P. G., Midtvedt, T., & Gordon, J. I. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.17.9833 · Cited by 500 · see citing works

A pneumococcal pilus influences virulence and host inflammatory responses

Barocchi, M. A., Ries, J., Zogaj, X., Hemsley, C. J., Albiger, B., Kanth, A., Dahlberg, S., Fernebro, J., Moschioni, M., Masignani, V., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511017103 · Cited by 474 · see citing works

Enhanced antiinflammatory capacity of a Lactobacillus plantarum mutant synthesizing modified teichoic acids

Grangette, C., Nutten, S., Palumbo, E., Morath, S., Hermann, C., Dewulf, J., Pot, B., Härtung, T., Pascal Hols, A., & Mercenier, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504084102 · Cited by 443 · see citing works

Human Intestinal Epithelial Cells Are Broadly Unresponsive to Toll-Like Receptor 2-Dependent Bacterial Ligands: Implications for Host-Microbial Interactions in the Gut

Melmed, G., Thomas, L. S., Lee, N., Tesfay, S. Y., Lukasek, K., Michelsen, K. S., Zhou, Y., Hu, B., Arditi, M., & Abreu, M. T. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.3.1406 · Cited by 431 · see citing works

Genomic and Metabolic Studies of the Impact of Probiotics on a Model Gut Symbiont and Host

Sonnenburg, J. L., Chen, C. T. L., & Gordon, J. I. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040413 · Cited by 423 · see citing works

Cell Surface-Associated Elongation Factor Tu Mediates the Attachment of <i>Lactobacillus johnsonii</i> NCC533 (La1) to Human Intestinal Cells and Mucins

Granato, D., Bergonzelli, G. E., Pridmore, R. D., Marvin, L., Rouvet, M., & Corthésy-Theulaz, I. E. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2160-2169.2004 · Cited by 410 · see citing works

Getting a grip on things: how do communities of bacterial symbionts become established in our intestine?

Sonnenburg, J. L., Angenent, L. T., & Gordon, J. I. (2004) · Nature Immunology · doi:10.1038/ni1079 · Cited by 406 · see citing works

Probiotics ameliorate the hydrogen peroxide-induced epithelial barrier disruption by a PKC- and MAP kinase-dependent mechanism

Seth, A., Yan, F., Polk, D. B., & Rao, R. K. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00202.2007 · Cited by 404 · see citing works

Probiotic lactobacilli and VSL#3 induce enterocyte β‐defensin 2

Schlee, M., Harder, J., Köten, B., Stange, E., Wehkamp, J., & Fellermann, K. (2008) · Clinical and Experimental Immunology · doi:10.1111/j.1365-2249.2007.03587.x · Cited by 393 · see citing works

A critical role for peptidoglycan N-deacetylation in Listeria evasion from the host innate immune system

Boneca, I. G., Dussurget, O., Cabanes, D., Nahori, M., Sousa, S., Lecuit, M., Psylinakis, E., Bouriotis, V., Hugot, J., Giovannini, M., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609672104 · Cited by 378 · see citing works

BACTERIAL INTERACTIONS WITH CELLS OF THE INTESTINAL MUCOSA: TOLL-LIKE RECEPTORS AND NOD2

Cario, E. (2005) · Gut · doi:10.1136/gut.2004.062794 · Cited by 350 · see citing works

Strategic Compartmentalization of Toll-Like Receptor 4 in the Mouse Gut

Ortega-Cava, C. F., Ishihara, S., Rumi, M. A. K., Kawashima, K., Ishimura, N., Kazumori, H., Udagawa, J., Kadowaki, Y., & Kinoshita, Y. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.8.3977 · Cited by 346 · see citing works

Towards understanding molecular modes of probiotic action

Marco, M. L., Pavan, S., & Kleerebezem, M. (2006) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2006.02.005 · Cited by 343 · see citing works

Helicobacter pylori Modulates the T Helper Cell 1/T Helper Cell 2 Balance through Phase-variable Interaction between Lipopolysaccharide and DC-SIGN

Bergman, M. P., Engering, A. J., Smits, H. H., van Vliet, S. J., Bodegraven, A. A. V., Wirth, H.-P., Kapsenberg, M. L., Vandenbroucke‐Grauls, C. M. J. E., van Kooyk, Y., & Appelmelk, B. J. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20041061 · Cited by 332 · see citing works

Lipoteichoic Acids from Lactobacillus Strains Elicit Strong Tumor Necrosis Factor Alpha-Inducing Activities in Macrophages through Toll-Like Receptor 2

Matsuguchi, T., Takagi, A., Matsuzaki, T., Nagaoka, M., Ishikawa, K., Yokokura, T., & Yoshikai, Y. (2003) · Clinical Diagnostic Laboratory Immunology · doi:10.1128/cdli.10.2.259-266.2003 · Cited by 328 · see citing works

Cathelicidins: a family of endogenous antimicrobial peptides

Lehrer, R. I., & Ganz, T. (2002) · Current Opinion in Hematology · doi:10.1097/00062752-200201000-00004 · Cited by 324 · see citing works

Biodiversity-Based Identification and Functional Characterization of the Mannose-Specific Adhesin of<i>Lactobacillus plantarum</i>

Pretzer, G., Snel, J., Molenaar, D., Wiersma, A., Bron, P. A., Lambert, J., de Vos, W. M., van der Meer, R., Smits, M. A., & Kleerebezem, M. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.17.6128-6136.2005 · Cited by 316 · see citing works

Induction of Human β-Defensin 2 by the ProbioticEscherichia coliNissle 1917 Is Mediated through Flagellin

Schlee, M., Wehkamp, J., Altenhoefer, A., Oelschlaeger, T. A., Stange, E. F., & Fellermann, K. (2007) · Infection and Immunity · doi:10.1128/iai.01563-06 · Cited by 315 · see citing works

GroEL of Lactobacillus johnsonii La1 (NCC 533) Is Cell Surface Associated: Potential Role in Interactions with the Host and the Gastric Pathogen Helicobacter pylori

Bergonzelli, G. E., Granato, D., Pridmore, R. D., Marvin, L., Donnicola, D., & Corthesy-Theulaz, I. E. (2005) · Infection and Immunity · doi:10.1128/iai.74.1.425-434.2006 · Cited by 302 · see citing works

The biosynthesis and functionality of the cell-wall of lactic acid bacteria.

Delcour, J., Ferain, T., Deghorain, M., Palumbo, E., & Pascal Hols, A. (1999) · PubMed · Cited by 286 · see citing works

A Key Role of Dendritic Cells in Probiotic Functionality

Foligné, B., Ζουμποπούλου, Γ., Dewulf, J., Younes‐Chennoufi, A. B., Chareyre, F., Sirard, J., Pot, B., & Grangette, C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000313 · Cited by 278 · see citing works

A bacterial carbohydrate links innate and adaptive responses through Toll-like receptor 2

Wang, Q., McLoughlin, R. M., Cobb, B. A., Charrel-Dennis, M., Zaleski, K. J., Golenbock, D. T., Tzianabos, A. O., & Kasper, D. L. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20062008 · Cited by 277 · see citing works

Identification of a Gene Cluster for the Biosynthesis of a Long, Galactose-Rich Exopolysaccharide in Lactobacillus rhamnosus GG and Functional Analysis of the Priming Glycosyltransferase

Lebeer, S., Verhoeven, T. L. A., Francius, G., Schoofs, G., Lambrichts, I., Dufrêne, Y. F., Vanderleyden, J., & Keersmaecker, S. C. J. D. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02919-08 · Cited by 271 · see citing works

Glycans as legislators of host-microbial interactions: spanning the spectrum from symbiosis to pathogenicity

Hooper, L. V., & Gordon, J. I. (2001) · Glycobiology · doi:10.1093/glycob/11.2.1r · Cited by 263 · see citing works

MD-2 and TLR4 N-Linked Glycosylations Are Important for a Functional Lipopolysaccharide Receptor

Correia, J. D. S., & Ulevitch, R. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109910200 · Cited by 262 · see citing works

The biosynthesis and functionality of the cell-wall of lactic acid bacteria

Delcour, J., Ferain, T., Deghorain, M., Palumbo, E., & Pascal Hols, A. (1999) · Antonie van Leeuwenhoek · doi:10.1023/a:1002089722581 · Cited by 262 · see citing works

Pseudomonas aeruginosa Flagella Activate Airway Epithelial Cells through asialoGM1 and Toll-Like Receptor 2 as well as Toll-Like Receptor 5

Adamo, R., Sokol, S., Soong, G., Gómez, M. I., & Prince, A. S. (2003) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2003-0260oc · Cited by 258 · see citing works

Do symbiotic bacteria subvert host immunity?

Hooper, L. V. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2114 · Cited by 256 · see citing works

hPepT1 transports muramyl dipeptide, activating NF-κB and stimulating IL-8 secretion in human colonic Caco2/bbe cells

Vavricka, S. R., Musch, M. W., Chang, J. E., Nakagawa, Y., Phanvijhitsiri, K., Waypa, T. S., Merlin, D., Schneewind, O., & Chang, E. B. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.07.024 · Cited by 243 · see citing works

Flagellin Is the Major Proinflammatory Determinant of Enteropathogenic Salmonella

Zeng, H., Carlson, A., Guo, Y., Yu, Y., Collier-Hyams, L. S., Madara, J., Gewirtz, A. T., & Neish, A. S. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.7.3668 · Cited by 235 · see citing works

Clinical Indications for Probiotics: An Overview

Goldin, B., & Gorbach, S. L. (2008) · Clinical Infectious Diseases · doi:10.1086/523333 · Cited by 231 · see citing works

Flagellar glycosylation – a new component of the motility repertoire?

Logan, S. M. (2006) · Microbiology · doi:10.1099/mic.0.28735-0 · Cited by 221 · see citing works

Vi polysaccharide of Salmonella typhi targets the prohibitin family of molecules in intestinal epithelial cells and suppresses early inflammatory responses

Sharma, A., & Qadri, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407536101 · Cited by 211 · see citing works

Never say never again: protein glycosylation in pathogenic bacteria

Benz, I., & Schmidt, M. A. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03030.x · Cited by 209 · see citing works

Pathogen induction of CXCR4/TLR2 cross-talk impairs host defense function

Hajishengallis, G., Wang, M., Liang, S., Triantafilou, M., & Triantafilou, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803852105 · Cited by 199 · see citing works

The Vi Capsular Antigen ofSalmonella entericaSerotype Typhi Reduces Toll-Like Receptor-Dependent Interleukin-8 Expression in the Intestinal Mucosa

Raffatellu, M., Chessa, D., Wilson, R. P., Dusold, R., Rubino, S., & Bäumler, A. J. (2005) · Infection and Immunity · doi:10.1128/iai.73.6.3367-3374.2005 · Cited by 196 · see citing works

In Vitro and ex Vivo Activation of the TLR5 Signaling Pathway in Intestinal Epithelial Cells by a Commensal Escherichia coli Strain

Bambou, J., Giraud, A., Ménard, S., Bègue, B., Rakotobé, S., Heyman, M., Taddéi, F., Cerf–Bensussan, N., & Gaboriau‐Routhiau, V. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m405410200 · Cited by 195 · see citing works

Pili with strong attachments: Gram‐positive bacteria do it differently

Scott, J. R., & Zähner, D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05279.x · Cited by 193 · see citing works

Lipopolysaccharides of Bacteroides fragilis, Chlamydia trachomatis and Pseudomonas aeruginosa signal via Toll-like receptor 2

Erridge, C., Pridmore, A. C., Eley, A., et al. (2004) · Journal of Medical Microbiology · doi:10.1099/jmm.0.45598-0 · Cited by 185 · see citing works

A conserved surface on Toll-like receptor 5 recognizes bacterial flagellin

Andersen‐Nissen, E., Smith, K. D., Bonneau, R., Strong, R. K., & Aderem, A. A. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061400 · Cited by 183 · see citing works

A Single Nucleotide Exchange in the wzy Gene Is Responsible for the Semirough O6 Lipopolysaccharide Phenotype and Serum Sensitivity of Escherichia coli Strain Nissle 1917

Grozdanov, L., Zähringer, U., Blum–Oehler, G., Brade, L., Henne, A., Knirel, Y. A., Schombel, U., Schulze, J., Sonnenborn, U., Gottschalk, G., et al. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.21.5912-5925.2002 · Cited by 180 · see citing works

Toll‐like receptor 2 and nucleotide‐binding oligomerization domain‐2 play divergent roles in the recognition of gut‐derived lactobacilli and bifidobacteria in dendritic cells

Zeuthen, L., Fink, L. N., & Frøkiær, H. (2008) · Immunology · doi:10.1111/j.1365-2567.2007.02800.x · Cited by 175 · see citing works

Mechanism of pathogen‐specific TLR4 activation in the mucosa: Fimbriae, recognition receptors and adaptor protein selection

Fischer, H., Yamamoto, M., Akira, S., et al. (2005) · European Journal of Immunology · doi:10.1002/eji.200535149 · Cited by 173 · see citing works

Type IV pili‐dependent gliding motility in the Gram‐positive pathogen Clostridium perfringens and other Clostridia

Varga, J. J., Nguyen, V., O'Brien, D. K., Rodgers, K., Walker, R. A., & Melville, S. B. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05414.x · Cited by 171 · see citing works

Cell surface Lactobacillus plantarum LA 318 glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH) adheres to human colonic mucin

Kinoshita, H., Uchida, H., Kawai, Y., Kawasaki, T., Wakahara, N., Matsuo, H., Watanabe, M., Kitazawa, H., Ohnuma, S., Miura, K., et al. (2008) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03679.x · Cited by 163 · see citing works

Lessons from the genomes of bifidobacteria

Klijn, A., Mercenier, A., & Arigoni, F. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2005.04.010 · Cited by 161 · see citing works

Cellular trafficking of lipoteichoic acid and Toll-like receptor 2 in relation to signaling; role of CD14 and CD36

Nilsen, N. J., Deininger, S., Nonstad, U., Skjeldal, F. M., Husebye, H., Rodionov, D., von Aulock, S., Härtung, T., Lien, E., Bakke, O., et al. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0907656 · Cited by 161 · see citing works

Induction of inflammation as a possible mechanism of probiotic effect in atopic eczema–dermatitis syndrome

Viljanen, M., Pohjavuori, E., Haahtela, T., Korpela, R., Kuitunen, M., Sarnesto, A., Vaarala, O., & Savilahti, E. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.03.047 · Cited by 157 · see citing works

F1C Fimbriae Play an Important Role in Biofilm Formation and Intestinal Colonization by the Escherichia coli Commensal Strain Nissle 1917

Lasaro, M. A., Salinger, N., Zhang, J., Wang, Y., Zhong, Z., Goulian, M., & Zhu, J. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.01144-08 · Cited by 153 · see citing works

Four N-linked Glycosylation Sites in Human Toll-like Receptor 2 Cooperate to Direct Efficient Biosynthesis and Secretion*

Weber, A., Morse, M., & Gay, N. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403830200 · Cited by 149 · see citing works

Probiotics as prevention and treatment for diarrhea

Guarino, A., Vecchio, A. L., & Canani, R. B. (2008) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e32831b4455 · Cited by 148 · see citing works

Multi-layered regulation of intestinal antimicrobial defense

Mukherjee, S., Vaishnava, S., & Hooper, L. V. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8182-3 · Cited by 146 · see citing works

Suppressive Effect on Activation of Macrophages by Lactobacillus casei Strain Shirota Genes Determining the Synthesis of Cell Wall-Associated Polysaccharides

Yasuda, E., Serata, M., & Sako, T. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00412-08 · Cited by 142 · see citing works

Induction of group A Streptococcus virulence by a human antimicrobial peptide

Gryllos, I., Tran-Winkler, H. J., Cheng, M., Chung, H., Bolcome, R. E., Lu, W., Lehrer, R. I., & Wessels, M. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803815105 · Cited by 139 · see citing works

Combinational clustering of receptors following stimulation by bacterial products determines lipopolysaccharide responses

Triantafilou, M., Brandenburg, K., Kusumoto, S., Fukase, K., Mackie, A. R., Seydel, U., & Triantafilou, K. (2004) · Biochemical Journal · doi:10.1042/bj20040172 · Cited by 134 · see citing works

Lessons from the genomes of bifidobacteria

Klijn, A., Mercenier, A., & Arigoni, F. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.fmrre.2005.04.010 · Cited by 128 · see citing works

Lipoteichoic Acids fromLactobacillus johnsoniiStrain La1 andLactobacillus acidophilusStrain La10 Antagonize the Responsiveness of Human Intestinal Epithelial HT29 Cells to Lipopolysaccharide and Gram-Negative Bacteria

Vidal, K., Donnet‐Hughes, A., & Granato, D. (2002) · Infection and Immunity · doi:10.1128/iai.70.4.2057-2064.2002 · Cited by 125 · see citing works

Functional Analysis of d -Alanylation of Lipoteichoic Acid in the Probiotic StrainLactobacillus rhamnosusGG

Vélez, M. P., Verhoeven, T. L. A., Draing, C., von Aulock, S., Pfitzenmaier, M., Geyer, A., Lambrichts, I., Grangette, C., Pot, B., Vanderleyden, J., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.02083-06 · Cited by 125 · see citing works

Live and Ultraviolet-Inactivated Lactobacillus Rhamnosus GG Decrease Flagellin-Induced Interleukin-8 Production in Caco-2 Cells

Lopez, M., Li, N., Kataria, J., Russell, M., & Neu, J. (2008) · Journal of Nutrition · doi:10.3945/jn.108.093658 · Cited by 124 · see citing works

Importance of Glycans to the Host-Bacteroides Mutualism in the Mammalian Intestine

Comstock, L. E. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.05.010 · Cited by 114 · see citing works

Lactobacillus crispatus M247-Derived H2O2 Acts as a Signal Transducing Molecule Activating Peroxisome Proliferator Activated Receptor-γ in the Intestinal Mucosa

Voltan, S., Martines, D., Elli, M., Brun, P., Longo, S., Porzionato, A., Macchi, V., Renata D'Incà, Scarpa, M., Palù, G., et al. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.07.007 · Cited by 111 · see citing works

Protective Mechanism of Epigallocatechin‐3‐Gallate against Helicobacter pylori‐Induced Gastric Epithelial Cytotoxicity via the Blockage of TLR‐4 Signaling

Lee, K., Yeo, M., Choue, J., Jin, J., Park, S., Cheong, J., Lee, K. J., Kim, J., & Hahm, K. (2004) · Helicobacter · doi:10.1111/j.1083-4389.2004.00281.x · Cited by 104 · see citing works

Binding and Cellular Activation Studies Reveal That Toll-like Receptor 2 Can Differentially Recognize Peptidoglycan from Gram-positive and Gram-negative Bacteria

Asong, J., Wolfert, M. A., Maiti, K. K., Miller, D. K., & Boons, G. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m806633200 · Cited by 103 · see citing works

Helicobacter pylori heat-shock protein 60 induces interleukin-8 via a Toll-like receptor (TLR)2 and mitogen-activated protein (MAP) kinase pathway in human monocytes

Zhao, Y., Yokota, K., Ayada, K., Yamamoto, Y., Okada, T., Shen, L., & Oguma, K. (2007) · Journal of Medical Microbiology · doi:10.1099/jmm.0.46882-0 · Cited by 103 · see citing works

Selection of probiotic bacteria for prevention of allergic diseases: immunomodulation of neonatal dendritic cells

Niers, L. E. M., Hoekstra, M. O., Timmerman, H. M., van Uden, N. O. P., de Graaff, P. M. A., Smits, H. H., Kimpen, J. L. L., & Rijkers, G. T. (2007) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2007.03421.x · Cited by 101 · see citing works

Listeria monocytogenes-Infected Human Dendritic Cells: Uptake and Host Cell Response

Kolb‐Mäurer, A., Gentschev, I., Fries, H.-W., et al. (2000) · Infection and Immunity · doi:10.1128/iai.68.6.3680-3688.2000 · Cited by 95 · see citing works

Bacterial Capsule -- Old Dogmas and New Tricks

Kasper, D. L. (1986) · The Journal of Infectious Diseases · doi:10.1093/infdis/153.3.407 · Cited by 91 · see citing works

Helicobacter pylori-mediated transcriptional regulation of the human beta-defensin 2 gene requires NF-kappaB

Wada, A., Ogushi, K., Kimura, T., et al. (2001) · Cellular Microbiology · doi:10.1046/j.1462-5822.2001.00096.x · Cited by 85 · see citing works

Genetic Analysis of Postpartum Measures of Luteal Activity in Dairy Cows

Petersson, K.-J., Berglund, B., Strandberg, E., Gustafsson, H., Flint, A. P. F., Woolliams, J. A., & Royal, M. D. (2007) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(07)72644-9 · Cited by 63 · see citing works

Theex vivoresponse of human intestinal mucosa to enteropathogenicEscherichia coliinfection

Schüller, S., Lucas, M., Kaper, J. B., Girón, J. A., & Phillips, A. D. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01275.x · Cited by 59 · see citing works

The K5 Capsule of Escherichia coli Strain Nissle 1917 Is Important in Mediating Interactions with Intestinal Epithelial Cells and Chemokine Induction

Hafez, M., Hayes, K. S., Goldrick, M., Warhurst, G., Grencis, R. K., & Roberts, I. S. (2009) · Infection and Immunity · doi:10.1128/iai.00040-09 · Cited by 58 · see citing works

Inhibitory effects of Lactobacillus plantarum lipoteichoic acid (LTA) on Staphylococcus aureus LTA-induced tumor necrosis factor-alpha production.

Kim, H. G., Lee, S. Y., Kim, N.-R., et al. (2008) · PubMed · Cited by 57 · see citing works

Salmonella typhimurium transcytoses flagellin via an SPI2-mediated vesicular transport pathway

Lyons, S., Wang, L., Casanova, J. E., et al. (2004) · Journal of Cell Science · doi:10.1242/jcs.01500 · Cited by 56 · see citing works

Helicobacter pylori Protein HP0175 Transactivates Epidermal Growth Factor Receptor through TLR4 in Gastric Epithelial Cells

Basu, S., Pathak, S. K., Chatterjee, G., Pathak, S., Basu, J., & Kundu, M. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m805053200 · Cited by 55 · see citing works

Gangliosides Act as Co-receptors for Salmonella enteritidis FliC and Promote FliC Induction of Human β-Defensin-2 Expression in Caco-2 Cells

Ogushi, K., Wada, A., Niidome, T., Okuda, T., Llanes, R., Nakayama, M., Nishi, Y., Kurazono, H., Smith, K. D., Aderem, A. A., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m307944200 · Cited by 54 · see citing works

Modification of the Structure of Peptidoglycan Is a Strategy To Avoid Detection by Nucleotide-Binding Oligomerization Domain Protein 1

Wolfert, M. A., Roychowdhury, A., & Boons, G. (2006) · Infection and Immunity · doi:10.1128/iai.01597-06 · Cited by 54 · see citing works

Regulation of the intestinal glycoprotein glycosylation during postnatal development: role of hormonal and nutritional factors

Biol, M.-C., & Louisot, P. (2003) · Biochimie · doi:10.1016/s0300-9084(03)00039-7 · Cited by 52 · see citing works

Flow Cytometric Testing of Green Fluorescent Protein-TaggedLactobacillus rhamnosusGG for Response to Defensins

Keersmaecker, S. C. J. D., Braeken, K., Verhoeven, T. L. A., Vélez, M. P., Lebeer, S., Vanderleyden, J., & Pascal Hols, A. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.02605-05 · Cited by 51 · see citing works

Intestinal epithelial cell signalling and host‐derived negative regulators under chronic inflammation: to be or not to be activated determines the balance towards commensal bacteria

Haller, D. (2006) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2006.00762.x · Cited by 48 · see citing works

Probiotic Escherichia coli Nissle 1917 Suppresses Allergen-Induced Th2 Responses in the Airways

Bickert, T., Trujillo-Vargas, C. M., Duechs, M. J., Wohlleben, G., Polte, T., Hansen, G., Oelschlaeger, T. A., & Erb, K. J. (2009) · International Archives of Allergy and Immunology · doi:10.1159/000199717 · Cited by 46 · see citing works

Innate Recognition of Bacteria: Engagement of Multiple Receptors

Triantafilou, M., Brandenburg, K., Gutsmann, T., et al. (2002) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.v22.i4.10 · Cited by 29 · see citing works

CD14: Chaperone or Matchmaker?

Finberg, R. W., & Kurt‐Jones, E. A. (2006) · Immunity · doi:10.1016/j.immuni.2006.01.010 · Cited by 26 · see citing works

Glycomics Aims To Interpret the Third Molecular Language of Cells

Weiss, A. A., & Iyer, S. S. (2007) · Microbe Magazine · doi:10.1128/microbe.2.489.1 · Cited by 10 · see citing works

The International Scientific Association of Probiotics and Prebiotics (ISAPP) Consensus Statement on the Definition and Scope of Postbiotics

Salminen, S., Collado, M. C., Endo, A., Hill, C., Lebeer, S., Quigley, E. M. M., Sanders, M. E., Shamir, R., Swann, J. R., Szajewska, H., et al. (2021) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/s41575-021-00440-6 · Cited by 2,488 · see citing works

The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on the definition and scope of synbiotics

Swanson, K. S., Gibson, G. R., Hutkins, R., Reimer, R. A., Reid, G., Verbeke, K., Scott, K. P., Holscher, H. D., Azad, M. B., Delzenne, N. M., et al. (2020) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/s41575-020-0344-2 · Cited by 2,196 · see citing works

The international scientific association for probiotics and prebiotics (ISAPP) consensus statement on fermented foods

Marco, M. L., Sanders, M. E., Gänzle, M., Arrieta, M. C., Cotter, P. D., De Vuyst, L., Hill, C., Holzapfel, W., Lebeer, S., Merenstein, D., et al. (2021) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/s41575-020-00390-5 · Cited by 937 · see citing works

Probiotic species in the modulation of gut microbiota: An overview

Azad, M. A. K., Sarker, M., Li, T., & Yin, J. (2018) · BioMed Research International · doi:10.1155/2018/9478630 · Cited by 803 · see citing works

Adhesion mechanisms mediated by probiotics and prebiotics and their potential impact on human health

Monteagudo-Mera, A., Rastall, R. A., Gibson, G. R., Charalampopoulos, D., & Chatzifragkou, A. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09978-7 · Cited by 743 · see citing works

The immunomodulatory properties of probiotic microorganisms beyond their viability (ghost probiotics: proposal of paraprobiotic concept)

Taverniti, V., & Guglielmetti, S. (2011) · Genes &amp; Nutrition · doi:10.1007/s12263-011-0218-x · Cited by 703 · see citing works

Emerging molecular insights into the interaction between probiotics and the host intestinal mucosa

Bron, P. A., van Baarlen, P., & Kleerebezem, M. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2690 · Cited by 690 · see citing works

Fate, activity, and impact of ingested bacteria within the human gut microbiota

Derrien, M., & van Hylckama Vlieg, J. E. T. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.03.002 · Cited by 605 · see citing works

Lactobacillus spp. for Gastrointestinal Health: Current and Future Perspectives

Dempsey, E., & Corr, S. C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.840245 · Cited by 579 · see citing works

Gut microbiota, obesity and diabetes

Patterson, E., Ryan, P. M., Cryan, J. F., Dinan, T. G., Ross, R. P., Fitzgerald, G. F., & Stanton, C. (2016) · Postgraduate Medical Journal · doi:10.1136/postgradmedj-2015-133285 · Cited by 552 · see citing works

An update on the use and investigation of probiotics in health and disease

Sanders, M. E., Guarner, F., Guerrant, R., Holt, P. R., Quigley, E. M., Sartor, R. B., Sherman, P. M., & Mayer, E. A. (2013) · Gut · doi:10.1136/gutjnl-2012-302504 · Cited by 503 · see citing works

Altered gut microbiota and activity in a murine model of autism spectrum disorders

de Theije, C. G. M., Wopereis, H., Ramadan, M., van Eijndthoven, T., Lambert, J., Knol, J., Garssen, J., Kraneveld, A. D., & Oozeer, R. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.005 · Cited by 433 · see citing works

Cell Wall Structure and Function in Lactic Acid Bacteria

Chapot-Chartier, M.-P., & Kulakauskas, S. (2014) · Microbial Cell Factories · doi:10.1186/1475-2859-13-s1-s9 · Cited by 410 · see citing works

Exopolysaccharides Produced by Lactic Acid Bacteria: From Health-Promoting Benefits to Stress Tolerance Mechanisms

Caggianiello, G., Kleerebezem, M., & Spano, G. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7471-2 · Cited by 396 · see citing works

Early life: gut microbiota and immune development in infancy

Martin, R., Nauta, A., Ben Amor, K., Knippels, L., Knol, J., & Garssen, J. (2010) · Beneficial Microbes · doi:10.3920/bm2010.0027 · Cited by 338 · see citing works

Microbiome in the gut-skin axis in atopic dermatitis

Lee, S.-Y., Lee, E., Park, Y. M., & Hong, S.-J. (2018) · Allergy, Asthma &amp; Immunology Research · doi:10.4168/aair.2018.10.4.354 · Cited by 326 · see citing works

Production of bioactive substances by intestinal bacteria as a basis for explaining probiotic mechanisms: Bacteriocins and conjugated linoleic acid

O'Shea, E. F., Cotter, P. D., Stanton, C., Ross, R. P., & Hill, C. (2012) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2011.05.025 · Cited by 305 · see citing works

Masquerading microbial pathogens: capsular polysaccharides mimic host-tissue molecules

Cress, B. F., Englaender, J. A., He, W., Kasper, D., Linhardt, R. J., & Koffas, M. A. G. (2014) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12056 · Cited by 282 · see citing works

International Society of Sports Nutrition Position Stand: Probiotics

Jäger, R., Mohr, A. E., Carpenter, K. C., Kerksick, C. M., Purpura, M., Moussa, A., Townsend, J. R., Lamprecht, M., West, N. P., Black, K., et al. (2019) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-019-0329-0 · Cited by 277 · see citing works

Exopolysaccharides as Antimicrobial Agents: Mechanism and Spectrum of Activity

Abdalla, A. K., Ayyash, M. M., Olaimat, A. N., Osaili, T. M., Al-Nabulsi, A. A., Shah, N. P., & Holley, R. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.664395 · Cited by 268 · see citing works

Probiotic <i>Lactobacillus</i> Strains Stimulate the Inflammatory Response and Activate Human Macrophages

Rocha-Ramírez, L. M., Pérez-Solano, R. A., Castañón-Alonso, S. L., Moreno Guerrero, S. S., Ramírez Pacheco, A., García Garibay, M., & Eslava, C. (2017) · Journal of Immunology Research · doi:10.1155/2017/4607491 · Cited by 227 · see citing works

Chronic obstructive pulmonary disease and asthma‐associated Proteobacteria, but not commensal <i>Prevotella</i> spp., promote <scp>T</scp>oll‐like receptor 2‐independent lung inflammation and pathology

Larsen, J. M., Musavian, H. S., Butt, T. M., Ingvorsen, C., Thysen, A. H., & Brix, S. (2015) · Immunology · doi:10.1111/imm.12376 · Cited by 200 · see citing works

Occurrence and Dynamism of Lactic Acid Bacteria in Distinct Ecological Niches: A Multifaceted Functional Health Perspective

George, F., Daniel, C., Thomas, M., Singer, E., Guilbaud, A., Tessier, F. J., Revol-Junelles, A.-M., Borges, F., & Foligné, B. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02899 · Cited by 198 · see citing works

The Relationship between the Structural Characteristics of Lactobacilli-EPS and Its Ability to Induce Apoptosis in Colon Cancer Cells in Vitro

Tukenmez, U., Aktas, B., Aslim, B., & Yavuz, S. (2019) · Scientific Reports · doi:10.1038/s41598-019-44753-8 · Cited by 167 · see citing works

Functional Dynamics of the Gut Microbiome in Elderly People during Probiotic Consumption

Eloe-Fadrosh, E. A., Brady, A., Crabtree, J., Drabek, E. F., Ma, B., Mahurkar, A., Ravel, J., Haverkamp, M., Fiorino, A.-M., Botelho, C., et al. (2015) · mBio · doi:10.1128/mbio.00231-15 · Cited by 160 · see citing works

Probiotics as an immune modulator

KANG, H.-J., & IM, S.-H. (2015) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.61.s103 · Cited by 151 · see citing works

Lactic Acid Bacteria Isolated from Bovine Mammary Microbiota: Potential Allies against Bovine Mastitis

Bouchard, D. S., Seridan, B., Saraoui, T., Rault, L., Germon, P., Gonzalez-Moreno, C., Nader-Macias, F. M. E., Baud, D., François, P., Chuat, V., et al. (2015) · PLOS ONE · doi:10.1371/journal.pone.0144831 · Cited by 144 · see citing works

Bifidobacterium bifidum: A Key Member of the Early Human Gut Microbiota

Turroni, F., Duranti, S., Milani, C., Lugli, G. A., van Sinderen, D., & Ventura, M. (2019) · Microorganisms · doi:10.3390/microorganisms7110544 · Cited by 140 · see citing works

Systems Solutions by Lactic Acid Bacteria: From Paradigms to Practice

de Vos, W. M. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-s1-s2 · Cited by 134 · see citing works

A Novel Extracellular Metallopeptidase Domain Shared by Animal Host-Associated Mutualistic and Pathogenic Microbes

Nakjang, S., Ndeh, D. A., Wipat, A., Bolam, D. N., & Hirt, R. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030287 · Cited by 116 · see citing works

How can probiotics and prebiotics impact mucosal immunity?

O'Flaherty, S., Saulnier, D., Pot, B., & Versalovic, J. (2010) · Gut Microbes · doi:10.4161/gmic.1.5.12924 · Cited by 103 · see citing works

Diverse action of lipoteichoic acid and lipopolysaccharide on neuroinflammation, blood-brain barrier disruption, and anxiety in mice

Mayerhofer, R., Fröhlich, E. E., Reichmann, F., Farzi, A., Kogelnik, N., Fröhlich, E., Sattler, W., & Holzer, P. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.10.011 · Cited by 89 · see citing works

<i>Lactobacillus rhamnosus</i> probiotic prevents airway function deterioration and promotes gut microbiome resilience in a murine asthma model

Spacova, I., Van Beeck, W., Seys, S., Devos, F., Vanoirbeek, J., Vanderleyden, J., Ceuppens, J., Petrova, M., & Lebeer, S. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1766345 · Cited by 87 · see citing works

Keeping <i>Candida</i> commensal: how lactobacilli antagonize pathogenicity of <i>Candida albicans</i> in an <i>in vitro</i> gut model

Graf, K., Last, A., Gratz, R., Allert, S., Linde, S., Westermann, M., Gröger, M., Mosig, A. S., Gresnigt, M. S., & Hube, B. (2019) · Disease Models &amp; Mechanisms · doi:10.1242/dmm.039719 · Cited by 83 · see citing works

Role of the intestinal microbiota in the immunomodulation of influenza virus infection

Chen, C.-J., Wu, G.-H., Kuo, R.-L., & Shih, S.-R. (2017) · Microbes and Infection · doi:10.1016/j.micinf.2017.09.002 · Cited by 67 · see citing works

The 2016 ESPEN Arvid Wretlind lecture: The gut in stress

McClave, S. A., Lowen, C. C., & Martindale, R. G. (2018) · Clinical Nutrition · doi:10.1016/j.clnu.2017.07.015 · Cited by 63 · see citing works

Pharmaconutrition Review: Physiological Mechanisms

Pierre, J. F., Heneghan, A. F., Lawson, C. M., Wischmeyer, P. E., Kozar, R. A., & Kudsk, K. A. (2013) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/0148607113493326 · Cited by 51 · see citing works

Recent advances in understanding of multifaceted changes in the vaginal microenvironment: implications in vaginal health and therapeutics

Das, S., Bhattacharjee, M. J., Mukherjee, A. K., & Khan, M. R. (2023) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2049696 · Cited by 51 · see citing works

Understanding and Modulating Mammalian-Microbial Communication for Improved Human Health

Mani, S., Boelsterli, U. A., & Redinbo, M. R. (2014) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011613-140007 · Cited by 48 · see citing works

The role of S-layer in adhesive and immunomodulating properties of probiotic starter culture Lactobacillus brevis D6 isolated from artisanal smoked fresh cheese

Uroić, K., Novak, J., Hynönen, U., Pietilä, T. E., Leboš Pavunc, A., Kant, R., Kos, B., Palva, A., & Šušković, J. (2016) · LWT - Food Science and Technology · doi:10.1016/j.lwt.2016.02.013 · Cited by 46 · see citing works

Probiotic supplementation has a limited effect on circulating immune and inflammatory markers in healthy adults: A systematic review of randomized controlled trials

Mohr, A. E., Basile, A. J., Crawford, M. S., Sweazea, K. L., & Carpenter, K. C. (2020) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2019.08.018 · Cited by 37 · see citing works

An Extracellular Serine/Threonine-Rich Protein from Lactobacillus plantarum NCIMB 8826 Is a Novel Aggregation-Promoting Factor with Affinity to Mucin

Hevia, A., Martínez, N., Ladero, V., Álvarez, M. A., Margolles, A., & Sánchez, B. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.01657-13 · Cited by 35 · see citing works

Antibacterial and Immunostimulatory Activity of Potential Probiotic Lactic Acid Bacteria Isolated from Ethiopian Fermented Dairy Products

Gizachew, S., Van Beeck, W., Spacova, I., Dekeukeleire, M., Alemu, A., Woldemedhin, W. M., Mariam, S. H., Lebeer, S., & Engidawork, E. (2023) · Fermentation · doi:10.3390/fermentation9030258 · Cited by 26 · see citing works

Unveiling The Therapeutic Potential of Probiotics: A Review

Tukaram, K. S., Sopanrao, S. R., & Kacharu, L. O. (2025) · Journal of Future Foods · doi:10.1016/j.jfutfo.2025.09.011 · Cited by 19 · see citing works

Characterization of S-layer proteins produced by lactobacilli isolated from Romanian artisan fermented products

Grosu-Tudor, S.-S., Angelescu, I.-R., Brînzan, A., & Zamfir, M. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxac063 · Cited by 9 · see citing works

Probiotic potential of Lactobacillus acidophilus TMPC 41127 isolated from traditional cheese in inhibiting Salmonella Typhi biofilms and virulence genes

Alizadeh Behbahani, B., Ghasemi, P., Vasiee, A., & Mousavi, Z. (2026) · Scientific Reports · doi:10.1038/s41598-026-51296-2 · Cited by 11 · see citing works

The role of teichoic acids of bifidobacteria in driving the interaction with the human host

Longhi, G., Vergna, L. M., Lugli, G. A., Bianchi, M. G., Tarracchini, C., Milani, C., Turroni, F., Bussolati, O., van Sinderen, D., & Ventura, M. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1616397 · Cited by 6 · see citing works

Probiotics: Origin, Products, and Regulations in India

Narula, A. (2021) · Microorganisms for Sustainability · doi:10.1007/978-981-16-1947-2_4 · Cited by 6 · see citing works

Bile resistance mechanisms in probiotics: From structural adaptation to metabolic regulation

Hu, J.-W., Guo, S.-J., Zhang, L.-W., & Guo, C.-F. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108282 · Cited by 5 · see citing works

[The history of commensalism: a contemporary history of microbiology].

Poreau, B. (2014) · PubMed · Cited by 2 · see citing works

Is absence of proof a proof of absence? Comments on commensalism

Zapalski, M. K. (2011) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2011.01.013 · Cited by 101 · see citing works

Molecular commensalism—how to investigate underappreciated health-associated polymicrobial communities

Labossiere, A., Ramsey, M. M., Merritt, J. L., & Kreth, J. (2023) · mBio · doi:10.1128/mbio.01342-23 · Cited by 6 · see citing works

Global Stability of Symbiotic Model of Commensalism and Parasitism with Harvesting in Commensal Populations

Chen, F., Zhou, Q., & Lin, S. (2022) · WSEAS TRANSACTIONS ON MATHEMATICS · doi:10.37394/23206.2022.21.50 · Cited by 9 · see citing works

USE OF TWO PROBIOTICS AND THEIR COMBINATION IN PRODUCTIVTY PERFORMANCE OF HY-LINE LAYERS

القزاز, M. F. A. A.-K. م. ف. ع. ا. (2009) · IRAQI JOURNAL OF AGRICULTURAL SCIENCES